geneid | 84188 |
---|---|
ensemblid | ENSG00000197601.14 |
hgncid | 26222 |
symbol | FAR1 |
name | fatty acyl-CoA reductase 1 |
refseq_nuc | NM_032228.6 |
refseq_prot | NP_115604.1 |
ensembl_nuc | ENST00000354817.8 |
ensembl_prot | ENSP00000346874.3 |
mane_status | MANE Select |
chr | chr11 |
start | 13668668 |
end | 13732346 |
strand | + |
ver | v1.2 |
region | chr11:13668668-13732346 |
region5000 | chr11:13663668-13737346 |
regionname0 | FAR1_chr11_13668668_13732346 |
regionname5000 | FAR1_chr11_13663668_13737346 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1548 | 345 | 90 | 59 | 137 | 16 | 41 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
c0002 | 0/0 | 1548 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
c0003 | 0/0 | 1548 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
c0004 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
c0005 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
c0006 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
c0007 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3719 | 96 | 14 | 16 | 51 | 4 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0002 | 0/1 | 3719 | 86 | 12 | 10 | 49 | 4 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0003 | 0/0 | 3718 | 84 | 28 | 16 | 26 | 5 | 9 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0004 | 0/0 | 3714 | 31 | 4 | 7 | 8 | 2 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0005 | 0/0 | 3713 | 9 | 8 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0006 | 0/0 | 3717 | 5 | 5 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0007 | 0/0 | 3718 | 4 | 4 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0008 | 0/0 | 3713 | 4 | 2 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0009 | 0/0 | 3721 | 3 | 2 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0010 | 0/0 | 3714 | 3 | 0 | 1 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0011 | 0/0 | 3713 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0012 | 0/0 | 3718 | 3 | 0 | 0 | 3 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0013 | 0/0 | 3718 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0014 | 0/0 | 3719 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0015 | 0/0 | 3718 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0016 | 0/0 | 3719 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0017 | 0/0 | 3718 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0018 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0019 | 0/0 | 3719 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0020 | 0/0 | 3719 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0021 | 0/0 | 3719 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0022 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0023 | 0/0 | 3719 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0024 | 0/0 | 3718 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0025 | 0/0 | 3718 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0026 | 0/0 | 3718 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0027 | 0/0 | 3718 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0028 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0029 | 0/0 | 3719 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
t0030 | 0/0 | 3719 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0003 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1548 | 345 | 90 | 59 | 137 | 16 | 41 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0002 | 0/0 | 1548 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0004 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0005 | 0/0 | 1548 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0006 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0007 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0002c0003 | 0/0 | 1548 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5266 | 95 | 14 | 16 | 50 | 4 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0002 | 0/1 | 5266 | 84 | 12 | 10 | 47 | 4 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0003 | 0/0 | 5265 | 83 | 28 | 16 | 26 | 5 | 8 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0004 | 0/0 | 5261 | 31 | 4 | 7 | 8 | 2 | 10 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0005 | 0/0 | 5260 | 9 | 8 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0006 | 0/0 | 5264 | 5 | 5 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0007 | 0/0 | 5265 | 4 | 4 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0008 | 0/0 | 5260 | 4 | 2 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0009 | 0/0 | 5268 | 3 | 2 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0011 | 0/0 | 5260 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0012 | 0/0 | 5265 | 3 | 0 | 0 | 3 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0013 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0014 | 0/0 | 5266 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0015 | 0/0 | 5265 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0016 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0017 | 0/0 | 5265 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0018 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0019 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0020 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0021 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0022 | 0/0 | 5264 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0023 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0024 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0025 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0026 | 0/0 | 5265 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0027 | 0/0 | 5265 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0028 | 0/0 | 5264 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0029 | 0/0 | 5266 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0001t0030 | 0/0 | 5266 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0002t0010 | 0/0 | 5261 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0004t0001 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0005t0003 | 0/0 | 5265 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0006t0002 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0001c0007t0002 | 0/0 | 5266 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
a0002c0003t0010 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | copy fasta | chr11 | 13663668 | 13737346 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0006g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0015g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0017g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0018g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0019g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0020g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0021g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0022g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0023g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0024g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0025g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0026g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0027g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0028g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0029g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0001t0030g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0002t0010g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0002t0010g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0005t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0006t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0001c0007t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
a0002c0003t0010g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0211 | EUR | GBR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00280 | hp1 | a0001 | c0001 | t0009 | g0255 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00558 | hp2 | a0001 | c0006 | t0002 | g0110 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00639 | hp1 | a0001 | c0001 | t0027 | g0040 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00642 | hp1 | a0002 | c0003 | t0010 | g0311 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0218 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01069 | hp1 | a0001 | c0001 | t0021 | g0008 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01069 | hp2 | a0001 | c0001 | t0029 | g0173 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0308 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01106 | hp1 | a0001 | c0001 | t0016 | g0094 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0288 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0299 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0219 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01255 | hp1 | a0001 | c0001 | t0024 | g0210 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01261 | hp1 | a0001 | c0001 | t0019 | g0015 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01261 | hp2 | a0001 | c0001 | t0018 | g0302 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01358 | hp1 | a0001 | c0001 | t0023 | g0091 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0024 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0024 | EUR | IBS | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0315 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02055 | hp2 | a0001 | c0001 | t0014 | g0163 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02257 | hp1 | a0001 | c0001 | t0013 | g0200 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0194 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0287 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0258 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0259 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0277 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02717 | hp1 | a0001 | c0001 | t0011 | g0280 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02738 | hp1 | a0001 | c0002 | t0010 | g0198 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0300 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02818 | hp2 | a0001 | c0001 | t0014 | g0073 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02886 | hp1 | a0001 | c0001 | t0015 | g0254 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0301 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0279 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0278 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0217 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0281 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0276 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03540 | hp2 | a0001 | c0001 | t0015 | g0253 | AFR | GWD | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03834 | hp1 | a0001 | c0002 | t0010 | g0310 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0289 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03942 | hp2 | a0001 | c0001 | t0030 | g0102 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0284 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04184 | hp1 | a0001 | c0001 | t0025 | g0215 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | BEB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0282 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0286 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0293 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | STU | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18946 | hp2 | a0001 | c0001 | t0017 | g0223 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18967 | hp1 | a0001 | c0007 | t0002 | g0165 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18969 | hp1 | a0001 | c0001 | t0022 | g0225 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18974 | hp1 | a0001 | c0004 | t0001 | g0156 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18982 | hp2 | a0001 | c0001 | t0012 | g0058 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18984 | hp2 | a0001 | c0001 | t0012 | g0129 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19002 | hp2 | a0001 | c0001 | t0020 | g0037 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20129 | hp1 | a0001 | c0001 | t0028 | g0039 | AFR | ASW | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ASW | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0206 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20905 | hp2 | a0001 | c0005 | t0003 | g0267 | SAS | GIH | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02109 | hp1 | a0001 | c0001 | t0026 | g0201 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0197 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0220 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | MSL | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18955 | hp1 | a0001 | c0001 | t0012 | g0154 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | USA | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0199 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | LWK | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0063 | REF | REF | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0038 | REF | REF | FAR1_chr11_13663668_13737346 | FAR1 | chr11 | 13663668 | 13737346 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:13700413
|
G | A | 1 | a0002 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.286G>A | p.Glu96Lys | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/12 | 432/5266 | 286/1548 | 96/515 | chr11 | 13700413 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:13710702
|
T | C | 1 | a0001c0004 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.555T>C | p.Asp185Asp | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 5/12 | 701/5266 | 555/1548 | 185/515 | chr11 | 13710702 | ||
chr11:13712020
|
G | A | 1 | a0001c0005 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.861G>A | p.Ala287Ala | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/12 | 1007/5266 | 861/1548 | 287/515 | chr11 | 13712020 | ||
chr11:13712987
|
T | C | 1 | a0001c0006 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.909T>C | p.Tyr303Tyr | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/12 | 1055/5266 | 909/1548 | 303/515 | chr11 | 13712987 | ||
chr11:13713008
|
T | C | 2 | a0001c0002a0002c0003 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
synonymous_variant | LOW | c.930T>C | p.Thr310Thr | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/12 | 1076/5266 | 930/1548 | 310/515 | chr11 | 13713008 | ||
chr11:13728708
|
C | T | 1 | a0001c0007 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.1482C>T | p.Tyr494Tyr | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1628/5266 | 1482/1548 | 494/515 | chr11 | 13728708 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:13668733
|
A | G | 1 | a0001c0001t0030 | 1 | HG03942.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/12 | 26033 | chr11 | 13668733 | |||||
chr11:13668752
|
C | CGCA | 1 | a0001c0001t0009 | 3 | HG00280.hp1 HG02622.hp2 HG02630.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59_-57dupAGC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/12 | 26008 | INFO_REALIGN_3_PRIME | chr11 | 13668752 | ||||
chr11:13668773
|
A | T | 1 | a0001c0001t0029 | 1 | HG01069.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-41A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/12 | chr11 | 13668773 | ||||||
chr11:13728803
|
A | G | 1 | a0001c0001t0015 | 2 | HG02886.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 29 | chr11 | 13728803 | |||||
chr11:13729044
|
A | G | 2 | a0001c0001t0027a0001c0001t0028 | 2 | HG00639.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 270 | chr11 | 13729044 | |||||
chr11:13729074
|
G | A | 1 | a0001c0001t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 300 | chr11 | 13729074 | |||||
chr11:13729328
|
TCTC | T | 2 | a0001c0002t0010a0002c0003t0010 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*555_*557delCTC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 555 | chr11 | 13729328 | |||||
chr11:13729334
|
TTTTC | T | 1 | a0001c0001t0008 | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*564_*567delCTTT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 564 | INFO_REALIGN_3_PRIME | chr11 | 13729334 | ||||
chr11:13729354
|
G | A | 2 | a0001c0001t0006a0001c0001t0007 | 9 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*580G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 580 | chr11 | 13729354 | |||||
chr11:13729399
|
A | C | 1 | a0001c0001t0026 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 625 | chr11 | 13729399 | |||||
chr11:13729414
|
T | C | 1 | a0001c0001t0013 | 2 | HG02257.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 640 | chr11 | 13729414 | |||||
chr11:13729433
|
G | A | 1 | a0001c0001t0017 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 659 | chr11 | 13729433 | |||||
chr11:13729841
|
T | C | 1 | a0001c0001t0011 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1067T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1067 | chr11 | 13729841 | |||||
chr11:13729919
|
G | A | 1 | a0001c0001t0018 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1145G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1145 | chr11 | 13729919 | |||||
chr11:13729958
|
A | G | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1184A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1184 | chr11 | 13729958 | |||||
chr11:13730228
|
ACTTT | A | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(1): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1459_*1462delCTTT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1459 | INFO_REALIGN_3_PRIME | chr11 | 13730228 | ||||
chr11:13730459
|
G | A | 1 | a0001c0001t0019 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1685 | chr11 | 13730459 | |||||
chr11:13730555
|
C | T | 1 | a0001c0001t0021 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1781C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 1781 | chr11 | 13730555 | |||||
chr11:13730812
|
A | T | 1 | a0001c0001t0025 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2038A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2038 | chr11 | 13730812 | |||||
chr11:13731010
|
G | C | 1 | a0001c0001t0015 | 2 | HG02886.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2236G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2236 | chr11 | 13731010 | |||||
chr11:13731059
|
T | G | 1 | a0001c0001t0008 | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2285T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2285 | chr11 | 13731059 | |||||
chr11:13731550
|
T | C | 1 | a0001c0001t0014 | 2 | HG02055.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2776T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 2776 | chr11 | 13731550 | |||||
chr11:13731830
|
A | G | 1 | a0001c0001t0024 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3056A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3056 | chr11 | 13731830 | |||||
chr11:13731939
|
G | A | 1 | a0001c0001t0020 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3165G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3165 | chr11 | 13731939 | |||||
chr11:13731988
|
C | G | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3214C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3214 | chr11 | 13731988 | |||||
chr11:13732070
|
A | G | 1 | a0001c0001t0008 | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3296A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3296 | chr11 | 13732070 | |||||
chr11:13732125
|
TA | T | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(11): Show | 135 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*3363delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3363 | INFO_REALIGN_3_PRIME | chr11 | 13732125 | ||||
chr11:13732125
|
TAA | T | 8 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(5): Show | 26 | HG00642.hp1 HG00735.hp1 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3362_*3363delAA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3362 | INFO_REALIGN_3_PRIME | chr11 | 13732125 | ||||
chr11:13732329
|
A | C | 1 | a0001c0001t0013 | 2 | HG02257.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3555A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 12/12 | 3555 | chr11 | 13732329 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:13668887
|
G | C | 1 | a0001c0001t0004g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8+81G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668887 | ||||||
chr11:13668901
|
G | C | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+95G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668901 | ||||||
chr11:13668938
|
C | A | 1 | a0001c0001t0001g0009 | 2 | HG00438.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-8+132C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668938 | ||||||
chr11:13668943
|
G | T | 1 | a0001c0001t0001g0316 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-8+137G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668943 | ||||||
chr11:13668983
|
G | A | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+177G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668983 | ||||||
chr11:13668992
|
C | T | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+186C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13668992 | ||||||
chr11:13669091
|
C | T | 1 | a0001c0001t0002g0025 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8+285C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669091 | ||||||
chr11:13669250
|
C | T | 2 | a0001c0002t0010g0310a0002c0003t0010g0311 | 2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+444C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669250 | ||||||
chr11:13669251
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8+445A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669251 | ||||||
chr11:13669884
|
TA | T | 156 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(153): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-8+1088delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13669884 | |||||
chr11:13669912
|
A | G | 1 | a0001c0001t0003g0308 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8+1106A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669912 | ||||||
chr11:13669963
|
G | A | 20 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0175others(17): Show | 20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8+1157G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13669963 | ||||||
chr11:13670307
|
G | T | 1 | a0001c0001t0003g0307 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8+1501G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670307 | ||||||
chr11:13670363
|
G | T | 1 | a0001c0001t0003g0306 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-8+1557G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670363 | ||||||
chr11:13670415
|
C | G | 41 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(38): Show | 43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8+1609C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670415 | ||||||
chr11:13670522
|
C | G | 3 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0305 | 3 | NA18953.hp2 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-8+1716C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670522 | ||||||
chr11:13670543
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0171 | 2 | NA18943.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-8+1737C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670543 | ||||||
chr11:13670549
|
C | T | 2 | a0001c0001t0002g0168a0001c0001t0003g0169 | 2 | NA18940.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-8+1743C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670549 | ||||||
chr11:13670647
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | NA18946.hp1 NA18951.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-8+1841T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670647 | ||||||
chr11:13670714
|
G | GT | 26 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0002g0166others(23): Show | 31 | HG00280.hp1 HG00423.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-8+1923dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13670714 | |||||
chr11:13670714
|
G | GTT | 20 | a0001c0001t0002g0025a0001c0001t0002g0174a0001c0001t0002g0175others(17): Show | 21 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+1922_-8+1923dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13670714 | |||||
chr11:13670724
|
T | A | 1 | a0001c0001t0001g0033 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-8+1918T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670724 | ||||||
chr11:13670945
|
T | C | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2139T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13670945 | ||||||
chr11:13671045
|
A | T | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+2239A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671045 | ||||||
chr11:13671289
|
A | G | 1 | a0001c0005t0003g0267 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+2483A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671289 | ||||||
chr11:13671374
|
A | G | 1 | a0001c0001t0003g0307 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8+2568A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671374 | ||||||
chr11:13671424
|
G | T | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+2618G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671424 | ||||||
chr11:13671976
|
T | A | 1 | a0001c0001t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8+3170T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13671976 | ||||||
chr11:13672388
|
C | CA | 16 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0002g0035others(13): Show | 18 | HG00642.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+3598dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672388 | |||||
chr11:13672388
|
C | CAA | 20 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(17): Show | 25 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+3597_-8+3598dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672388 | |||||
chr11:13672393
|
A | AT | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+3587_-8+3588ins others(1): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672393 | ||||||
chr11:13672399
|
A | T | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+3593A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672399 | ||||||
chr11:13672404
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-8+3598A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672404 | ||||||
chr11:13672504
|
C | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+3698C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672504 | ||||||
chr11:13672544
|
C | CA | 58 | a0001c0001t0001g0316a0001c0001t0003g0027a0001c0001t0003g0203others(55): Show | 62 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-8+3754dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672544 | |||||
chr11:13672544
|
C | CAA | 17 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(14): Show | 22 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8+3753_-8+3754dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13672544 | |||||
chr11:13672560
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8+3754A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672560 | ||||||
chr11:13672663
|
AG | A | 16 | a0001c0001t0002g0208a0001c0001t0003g0019a0001c0001t0003g0020others(13): Show | 18 | HG00140.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+3858delG | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672663 | ||||||
chr11:13672681
|
C | T | 50 | a0001c0001t0002g0208a0001c0001t0002g0229a0001c0001t0002g0246others(47): Show | 52 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-8+3875C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672681 | ||||||
chr11:13672830
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+4024A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672830 | ||||||
chr11:13672861
|
T | G | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+4055T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13672861 | ||||||
chr11:13673033
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8+4227C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673033 | ||||||
chr11:13673056
|
A | G | 308 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(305): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.-8+4250A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673056 | ||||||
chr11:13673239
|
G | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+4433G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673239 | ||||||
chr11:13673241
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+4435G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673241 | ||||||
chr11:13673377
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+4571T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673377 | ||||||
chr11:13673435
|
T | A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+4629T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13673435 | ||||||
chr11:13674047
|
C | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+5241C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674047 | ||||||
chr11:13674087
|
G | A | 1 | a0001c0001t0004g0268 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-8+5281G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674087 | ||||||
chr11:13674115
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+5309G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674115 | ||||||
chr11:13674165
|
C | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(48): Show | 57 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.-8+5359C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674165 | ||||||
chr11:13674266
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+5460G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674266 | ||||||
chr11:13674294
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-8+5488G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674294 | ||||||
chr11:13674303
|
C | T | 3 | a0001c0001t0003g0027a0001c0001t0013g0199a0001c0001t0013g0200 | 3 | HG01884.hp1 HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+5497C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674303 | ||||||
chr11:13674308
|
CA | C | 7 | a0001c0001t0001g0162a0001c0001t0002g0120a0001c0001t0002g0121others(4): Show | 7 | HG00323.hp2 HG02897.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+5518delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13674308 | |||||
chr11:13674320
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-8+5514A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674320 | ||||||
chr11:13674342
|
A | G | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+5536A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674342 | ||||||
chr11:13674349
|
C | T | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+5543C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674349 | ||||||
chr11:13674362
|
G | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-8+5556G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674362 | ||||||
chr11:13674500
|
A | G | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+5694A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674500 | ||||||
chr11:13674810
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18944.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-8+6004T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674810 | ||||||
chr11:13674826
|
A | G | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+6020A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674826 | ||||||
chr11:13674929
|
A | G | 7 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029others(4): Show | 9 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+6123A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13674929 | ||||||
chr11:13675053
|
C | CT | 251 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(248): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.-8+6262dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13675053 | |||||
chr11:13675053
|
C | CTT | 41 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(38): Show | 43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8+6261_-8+6262dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13675053 | |||||
chr11:13675103
|
TA | T | 53 | a0001c0001t0002g0208a0001c0001t0002g0229a0001c0001t0002g0246others(50): Show | 55 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.-8+6299delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13675103 | |||||
chr11:13675317
|
C | G | 35 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(32): Show | 36 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-8+6511C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675317 | ||||||
chr11:13675396
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+6590A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675396 | ||||||
chr11:13675439
|
G | T | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+6633G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675439 | ||||||
chr11:13675440
|
C | T | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+6634C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675440 | ||||||
chr11:13675441
|
T | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+6635T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675441 | ||||||
chr11:13675574
|
C | T | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0166 | 3 | HG03669.hp2 HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-8+6768C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675574 | ||||||
chr11:13675666
|
T | C | 2 | a0001c0001t0004g0026a0001c0001t0004g0275 | 2 | HG02027.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-8+6860T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675666 | ||||||
chr11:13675930
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-8+7124A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13675930 | ||||||
chr11:13676159
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8+7353G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676159 | ||||||
chr11:13676422
|
G | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-8+7616G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676422 | ||||||
chr11:13676569
|
A | C | 3 | a0001c0001t0002g0189a0001c0001t0002g0191a0001c0001t0029g0173 | 3 | HG00323.hp1 HG01069.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.-8+7763A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676569 | ||||||
chr11:13676598
|
G | A | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+7792G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676598 | ||||||
chr11:13676701
|
C | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+7895C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13676701 | ||||||
chr11:13677037
|
C | T | 2 | a0001c0002t0010g0310a0002c0003t0010g0311 | 2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+8231C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677037 | ||||||
chr11:13677056
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-8+8250A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677056 | ||||||
chr11:13677117
|
A | G | 4 | a0001c0001t0003g0227a0001c0001t0003g0250a0001c0001t0003g0251others(1): Show | 4 | HG02074.hp2 HG02523.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+8311A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677117 | ||||||
chr11:13677136
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-8+8330A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677136 | ||||||
chr11:13677286
|
A | G | 58 | a0001c0001t0002g0168a0001c0001t0002g0208a0001c0001t0002g0229others(55): Show | 60 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+8480A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677286 | ||||||
chr11:13677582
|
C | T | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+8776C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677582 | ||||||
chr11:13677656
|
C | T | 7 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0261others(4): Show | 11 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+8850C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677656 | ||||||
chr11:13677678
|
A | C | 1 | a0001c0001t0007g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-8+8872A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677678 | ||||||
chr11:13677826
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18954.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-8+9020A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677826 | ||||||
chr11:13677994
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-8+9188G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13677994 | ||||||
chr11:13678266
|
A | G | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8+9460A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678266 | ||||||
chr11:13678288
|
T | TGAGTCTC others(234): Show |
1 | a0001c0001t0001g0158 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8+9584_-8+9585ins others(241): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13678288 | |||||
chr11:13678486
|
G | A | 1 | a0001c0001t0005g0192 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8+9680G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678486 | ||||||
chr11:13678621
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+9815T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678621 | ||||||
chr11:13678703
|
C | T | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+9897C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678703 | ||||||
chr11:13678722
|
G | GT | 59 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0003g0003others(56): Show | 66 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-8+9917dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13678722 | |||||
chr11:13678724
|
C | T | 156 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(153): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-8+9918C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13678724 | ||||||
chr11:13679010
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0128 | 2 | NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-8+10204G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679010 | ||||||
chr11:13679062
|
ATATTT | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0175a0001c0001t0002g0176 | 3 | HG02647.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+10260_-8+10264d others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13679062 | |||||
chr11:13679092
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8+10286G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679092 | ||||||
chr11:13679178
|
A | T | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+10372A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679178 | ||||||
chr11:13679213
|
A | AC | 158 | a0001c0001t0002g0025a0001c0001t0002g0168a0001c0001t0002g0172others(155): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-8+10407_-8+10408i others(3): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679213 | ||||||
chr11:13679383
|
A | C | 1 | a0001c0001t0004g0297 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-8+10577A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679383 | ||||||
chr11:13679466
|
C | T | 4 | a0001c0001t0002g0186a0001c0001t0002g0189a0001c0001t0002g0191others(1): Show | 4 | HG00323.hp1 HG01069.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+10660C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679466 | ||||||
chr11:13679568
|
A | G | 1 | a0001c0001t0008g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8+10762A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679568 | ||||||
chr11:13679726
|
G | A | 1 | a0001c0002t0010g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-8+10920G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679726 | ||||||
chr11:13679734
|
A | G | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+10928A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679734 | ||||||
chr11:13679927
|
G | A | 1 | a0001c0001t0003g0228 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-8+11121G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679927 | ||||||
chr11:13679940
|
G | C | 2 | a0001c0001t0002g0057a0001c0001t0002g0115 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-8+11134G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679940 | ||||||
chr11:13679940
|
G | T | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+11134G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13679940 | ||||||
chr11:13680034
|
A | G | 1 | a0001c0001t0025g0215 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8+11228A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680034 | ||||||
chr11:13680098
|
T | C | 4 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(1): Show | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+11292T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680098 | ||||||
chr11:13680110
|
T | C | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+11304T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680110 | ||||||
chr11:13680228
|
CTCTT | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-8+11424_-8+11427d others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13680228 | |||||
chr11:13680315
|
A | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-8+11509A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680315 | ||||||
chr11:13680320
|
T | C | 1 | a0001c0001t0003g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-8+11514T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680320 | ||||||
chr11:13680787
|
T | C | 1 | a0001c0001t0012g0058 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-8+11981T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680787 | ||||||
chr11:13680808
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+12002G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680808 | ||||||
chr11:13680813
|
T | C | 8 | a0001c0001t0001g0059a0001c0001t0002g0001a0001c0001t0002g0011others(5): Show | 12 | NA18939.hp2 NA18954.hp2 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+12007T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680813 | ||||||
chr11:13680837
|
G | C | 93 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(90): Show | 102 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-8+12031G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13680837 | ||||||
chr11:13681184
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-8+12378G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681184 | ||||||
chr11:13681270
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8+12464G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681270 | ||||||
chr11:13681475
|
G | A | 7 | a0001c0001t0005g0023a0001c0001t0005g0192a0001c0001t0005g0269others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+12669G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681475 | ||||||
chr11:13681524
|
A | G | 1 | a0001c0001t0003g0314 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8+12718A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681524 | ||||||
chr11:13681559
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-8+12753A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681559 | ||||||
chr11:13681682
|
A | G | 1 | a0001c0001t0003g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-8+12876A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681682 | ||||||
chr11:13681894
|
T | A | 21 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(18): Show | 22 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-12865T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681894 | ||||||
chr11:13681904
|
T | C | 2 | a0001c0001t0027g0040a0001c0001t0028g0039 | 2 | HG00639.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-7-12855T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681904 | ||||||
chr11:13681973
|
T | A | 1 | a0001c0001t0003g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-7-12786T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681973 | ||||||
chr11:13681979
|
C | G | 1 | a0001c0001t0004g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-7-12780C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13681979 | ||||||
chr11:13682108
|
T | C | 20 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0175others(17): Show | 20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-12651T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682108 | ||||||
chr11:13682140
|
G | A | 35 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0027others(32): Show | 40 | HG00280.hp1 HG00642.hp1 HG01516.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7-12619G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682140 | ||||||
chr11:13682327
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0012g0129 | 2 | NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-7-12432T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682327 | ||||||
chr11:13682374
|
C | G | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7-12385C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682374 | ||||||
chr11:13682644
|
TGTCACCC others(8540): Show |
T | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-12113_-7-3567de others(1): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13682644 | |||||
chr11:13682875
|
G | A | 3 | a0001c0001t0002g0229a0001c0001t0003g0222a0001c0001t0003g0230 | 3 | NA18940.hp1 NA18962.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-7-11884G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13682875 | ||||||
chr11:13683187
|
G | A | 1 | a0001c0001t0004g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-7-11572G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683187 | ||||||
chr11:13683253
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-7-11506C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683253 | ||||||
chr11:13683306
|
T | C | 1 | a0001c0001t0025g0215 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7-11453T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683306 | ||||||
chr11:13683322
|
G | A | 9 | a0001c0001t0002g0042a0001c0001t0003g0010a0001c0001t0003g0041others(6): Show | 10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-11437G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683322 | ||||||
chr11:13683329
|
G | A | 1 | a0001c0001t0007g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-7-11430G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683329 | ||||||
chr11:13683350
|
A | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-11409A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683350 | ||||||
chr11:13683468
|
A | T | 3 | a0001c0001t0003g0022a0001c0001t0003g0261a0001c0001t0003g0262 | 4 | HG01884.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-11291A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683468 | ||||||
chr11:13683518
|
G | A | 1 | a0001c0001t0004g0277 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-11241G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683518 | ||||||
chr11:13683541
|
GT | G | 13 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0256others(10): Show | 15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-11209delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13683541 | |||||
chr11:13683601
|
G | A | 1 | a0001c0001t0002g0063 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-7-11158G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683601 | ||||||
chr11:13683745
|
G | GA | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-11008dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13683745 | |||||
chr11:13683761
|
G | A | 13 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0256others(10): Show | 15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-10998G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13683761 | ||||||
chr11:13684196
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-7-10563G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684196 | ||||||
chr11:13684283
|
TA | T | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-10473delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13684283 | |||||
chr11:13684364
|
G | C | 1 | a0001c0001t0004g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-10395G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684364 | ||||||
chr11:13684414
|
G | C | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-10345G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684414 | ||||||
chr11:13684513
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-7-10246T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684513 | ||||||
chr11:13684733
|
T | C | 1 | a0001c0001t0015g0253 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-7-10026T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13684733 | ||||||
chr11:13685042
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-7-9717A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685042 | ||||||
chr11:13685219
|
C | T | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-9540C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685219 | ||||||
chr11:13685283
|
A | AT | 6 | a0001c0001t0001g0157a0001c0001t0003g0027a0001c0001t0003g0245others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-9463dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13685283 | |||||
chr11:13685291
|
T | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-9468T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685291 | ||||||
chr11:13685292
|
T | G | 7 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(4): Show | 7 | HG00642.hp1 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-9467T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685292 | ||||||
chr11:13685293
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-7-9466T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685293 | ||||||
chr11:13685294
|
T | G | 3 | a0001c0001t0001g0066a0001c0001t0015g0253a0001c0001t0015g0254 | 3 | HG02886.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-9465T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685294 | ||||||
chr11:13685395
|
C | T | 1 | a0001c0001t0003g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7-9364C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685395 | ||||||
chr11:13685482
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-9277A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685482 | ||||||
chr11:13685769
|
A | C | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8990A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685769 | ||||||
chr11:13685932
|
A | G | 60 | a0001c0001t0001g0059a0001c0001t0001g0088a0001c0001t0002g0001others(57): Show | 71 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7-8827A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13685932 | ||||||
chr11:13686368
|
T | C | 1 | a0001c0001t0003g0312 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-7-8391T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686368 | ||||||
chr11:13686449
|
T | C | 1 | a0001c0001t0013g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-8310T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686449 | ||||||
chr11:13686495
|
C | T | 2 | a0001c0001t0003g0227a0001c0001t0005g0192 | 2 | HG02622.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.-7-8264C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686495 | ||||||
chr11:13686615
|
CTG | C | 7 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029others(4): Show | 9 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-8141_-7-8140del others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13686615 | |||||
chr11:13686685
|
T | C | 1 | a0001c0001t0003g0313 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-7-8074T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686685 | ||||||
chr11:13686717
|
TA | T | 309 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(306): Show | 342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-8034delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13686717 | |||||
chr11:13686948
|
C | T | 21 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(18): Show | 22 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-7811C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13686948 | ||||||
chr11:13687336
|
T | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-7423T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687336 | ||||||
chr11:13687383
|
G | A | 1 | a0001c0001t0003g0231 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-7-7376G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687383 | ||||||
chr11:13687591
|
C | T | 2 | a0001c0001t0003g0243a0001c0001t0003g0244 | 2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-7-7168C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687591 | ||||||
chr11:13687605
|
C | G | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-7154C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687605 | ||||||
chr11:13687767
|
G | A | 1 | a0001c0001t0026g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-6992G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687767 | ||||||
chr11:13687829
|
C | T | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-6930C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687829 | ||||||
chr11:13687869
|
C | T | 1 | a0001c0001t0004g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-6890C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687869 | ||||||
chr11:13687961
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-7-6798A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13687961 | ||||||
chr11:13688041
|
T | C | 1 | a0001c0001t0001g0316 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-7-6718T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688041 | ||||||
chr11:13688177
|
C | CA | 14 | a0001c0001t0005g0023a0001c0001t0005g0192a0001c0001t0005g0269others(11): Show | 17 | HG02145.hp2 HG02486.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-6573dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13688177 | |||||
chr11:13688185
|
A | T | 6 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0002g0122others(3): Show | 6 | HG00558.hp2 HG02027.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-6574A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688185 | ||||||
chr11:13688187
|
T | A | 39 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(36): Show | 45 | HG00280.hp1 HG00642.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.-7-6572T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688187 | ||||||
chr11:13688243
|
T | G | 1 | a0001c0001t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7-6516T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688243 | ||||||
chr11:13688251
|
TC | T | 132 | a0001c0001t0001g0032a0001c0001t0002g0208a0001c0001t0002g0246others(129): Show | 143 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.-7-6504delC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13688251 | |||||
chr11:13688252
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-7-6507C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688252 | ||||||
chr11:13688307
|
A | C | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-7-6452A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688307 | ||||||
chr11:13688333
|
A | G | 1 | a0001c0001t0003g0314 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7-6426A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688333 | ||||||
chr11:13688368
|
G | C | 1 | a0001c0001t0001g0013 | 2 | HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-7-6391G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688368 | ||||||
chr11:13688530
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-6229A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688530 | ||||||
chr11:13688564
|
T | C | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-6195T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688564 | ||||||
chr11:13688620
|
G | A | 7 | a0001c0001t0005g0023a0001c0001t0005g0192a0001c0001t0005g0269others(4): Show | 8 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-6139G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688620 | ||||||
chr11:13688655
|
A | G | 1 | a0001c0001t0003g0242 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-7-6104A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688655 | ||||||
chr11:13688821
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-7-5938G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13688821 | ||||||
chr11:13689144
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7-5615T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689144 | ||||||
chr11:13689193
|
T | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-5566T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689193 | ||||||
chr11:13689263
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-5496A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689263 | ||||||
chr11:13689682
|
G | A | 1 | a0001c0001t0026g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-5077G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689682 | ||||||
chr11:13689796
|
G | T | 27 | a0001c0001t0004g0024a0001c0001t0004g0268a0001c0001t0004g0275others(24): Show | 28 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7-4963G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689796 | ||||||
chr11:13689869
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-7-4890C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13689869 | ||||||
chr11:13689873
|
C | CT | 74 | a0001c0001t0001g0054a0001c0001t0001g0086a0001c0001t0001g0124others(71): Show | 79 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-7-4866dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13689873 | |||||
chr11:13689873
|
CT | C | 50 | a0001c0001t0002g0089a0001c0001t0004g0024a0001c0001t0004g0026others(47): Show | 52 | HG00544.hp2 HG00733.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-7-4866delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13689873 | |||||
chr11:13690303
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-4456G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690303 | ||||||
chr11:13690465
|
G | A | 34 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(31): Show | 35 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-7-4294G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690465 | ||||||
chr11:13690611
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-7-4148C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690611 | ||||||
chr11:13690769
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-7-3990G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690769 | ||||||
chr11:13690866
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-7-3893G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13690866 | ||||||
chr11:13691001
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7-3758C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691001 | ||||||
chr11:13691685
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-7-3074G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691685 | ||||||
chr11:13691836
|
C | A | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-2923C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691836 | ||||||
chr11:13691874
|
T | G | 16 | a0001c0001t0002g0208a0001c0001t0003g0019a0001c0001t0003g0020others(13): Show | 18 | HG00140.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7-2885T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13691874 | ||||||
chr11:13692247
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-7-2512A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692247 | ||||||
chr11:13692300
|
A | G | 9 | a0001c0001t0003g0021a0001c0001t0003g0256a0001c0001t0003g0257others(6): Show | 10 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-2459A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692300 | ||||||
chr11:13692316
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-7-2443G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692316 | ||||||
chr11:13692322
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-7-2437C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692322 | ||||||
chr11:13692544
|
TA | T | 20 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0175others(17): Show | 20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-2214delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692544 | ||||||
chr11:13692596
|
G | C | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-2163G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692596 | ||||||
chr11:13692641
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA18944.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-7-2118T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692641 | ||||||
chr11:13692695
|
A | G | 28 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(25): Show | 31 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-7-2064A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692695 | ||||||
chr11:13692820
|
A | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0126a0001c0001t0001g0148others(6): Show | 9 | HG02027.hp1 HG02083.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-1939A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692820 | ||||||
chr11:13692824
|
A | C | 1 | a0001c0001t0005g0192 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7-1935A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692824 | ||||||
chr11:13692902
|
G | C | 2 | a0001c0001t0003g0314a0001c0001t0003g0315 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-7-1857G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13692902 | ||||||
chr11:13693099
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-7-1660A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693099 | ||||||
chr11:13693262
|
A | C | 2 | a0001c0001t0003g0263a0001c0001t0003g0264 | 2 | HG01109.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-7-1497A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693262 | ||||||
chr11:13693295
|
C | T | 21 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(18): Show | 22 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-1464C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693295 | ||||||
chr11:13693359
|
CTTTTGTT others(3): Show |
C | 9 | a0001c0001t0002g0042a0001c0001t0003g0010a0001c0001t0003g0041others(6): Show | 10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-1390_-7-1381del others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13693359 | |||||
chr11:13693403
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-7-1356C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693403 | ||||||
chr11:13693432
|
C | T | 1 | a0001c0001t0007g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-7-1327C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693432 | ||||||
chr11:13693532
|
A | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-7-1227A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693532 | ||||||
chr11:13693577
|
CT | C | 52 | a0001c0001t0001g0059a0001c0001t0002g0001a0001c0001t0002g0002others(49): Show | 63 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-7-1178delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 13693577 | |||||
chr11:13693742
|
A | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-1017A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693742 | ||||||
chr11:13693834
|
T | A | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-7-925T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693834 | ||||||
chr11:13693892
|
A | C | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-867A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13693892 | ||||||
chr11:13694102
|
T | C | 77 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(74): Show | 86 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.-7-657T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694102 | ||||||
chr11:13694291
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-468A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694291 | ||||||
chr11:13694525
|
G | A | 3 | a0001c0001t0003g0027a0001c0001t0013g0199a0001c0001t0013g0200 | 3 | HG01884.hp1 HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-234G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694525 | ||||||
chr11:13694635
|
G | A | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-7-124G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694635 | ||||||
chr11:13694696
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-7-63T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694696 | ||||||
chr11:13694732
|
A | G | 2 | a0001c0001t0005g0269a0001c0001t0005g0298 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-7-27A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 1/11 | chr11 | 13694732 | ||||||
chr11:13694983
|
A | G | 158 | a0001c0001t0002g0025a0001c0001t0002g0168a0001c0001t0002g0172others(155): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.189+29A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13694983 | ||||||
chr11:13695067
|
T | TA | 45 | a0001c0001t0003g0003a0001c0001t0003g0263a0001c0001t0003g0264others(42): Show | 50 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.189+117dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13695067 | |||||
chr11:13695072
|
C | A | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.189+118C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695072 | ||||||
chr11:13695235
|
GTTGT | G | 4 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(1): Show | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+286_189+289del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13695235 | |||||
chr11:13695330
|
T | A | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189+376T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695330 | ||||||
chr11:13695737
|
G | A | 2 | a0001c0001t0001g0088a0001c0005t0003g0267 | 2 | NA18906.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.189+783G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695737 | ||||||
chr11:13695990
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.189+1036C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13695990 | ||||||
chr11:13696144
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.189+1190A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696144 | ||||||
chr11:13696347
|
T | G | 1 | a0001c0001t0003g0312 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189+1393T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696347 | ||||||
chr11:13696353
|
A | G | 1 | a0001c0001t0006g0029 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.189+1399A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696353 | ||||||
chr11:13696641
|
GACTTA | G | 49 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(46): Show | 53 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+1692_189+1696d others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13696641 | |||||
chr11:13696743
|
TATGTATA others(3): Show |
T | 1 | a0001c0001t0003g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189+1790_189+1799d others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696743 | ||||||
chr11:13696830
|
T | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189+1876T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696830 | ||||||
chr11:13696834
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.189+1880G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13696834 | ||||||
chr11:13697282
|
G | T | 1 | a0001c0001t0026g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.189+2328G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697282 | ||||||
chr11:13697321
|
G | A | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG02145.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.189+2367G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697321 | ||||||
chr11:13697401
|
G | T | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189+2447G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697401 | ||||||
chr11:13697423
|
C | G | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+2469C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697423 | ||||||
chr11:13697553
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.189+2599G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697553 | ||||||
chr11:13697865
|
T | A | 158 | a0001c0001t0002g0025a0001c0001t0002g0168a0001c0001t0002g0172others(155): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.190-2452T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697865 | ||||||
chr11:13697975
|
T | G | 310 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(307): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.190-2342T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697975 | ||||||
chr11:13697995
|
C | G | 2 | a0001c0001t0003g0314a0001c0001t0003g0315 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.190-2322C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13697995 | ||||||
chr11:13698059
|
A | G | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-2258A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698059 | ||||||
chr11:13698319
|
C | T | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.190-1998C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698319 | ||||||
chr11:13698357
|
T | C | 1 | a0001c0001t0004g0281 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190-1960T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698357 | ||||||
chr11:13698408
|
A | G | 1 | a0001c0001t0002g0025 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.190-1909A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698408 | ||||||
chr11:13698435
|
A | G | 1 | a0001c0001t0007g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190-1882A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698435 | ||||||
chr11:13698553
|
C | T | 1 | a0001c0001t0003g0240 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.190-1764C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698553 | ||||||
chr11:13698602
|
G | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.190-1715G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698602 | ||||||
chr11:13698626
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190-1691C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698626 | ||||||
chr11:13698691
|
C | T | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.190-1626C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698691 | ||||||
chr11:13698780
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.190-1537G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698780 | ||||||
chr11:13698785
|
C | T | 41 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(38): Show | 43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.190-1532C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698785 | ||||||
chr11:13698806
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.190-1511G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698806 | ||||||
chr11:13698830
|
C | CA | 9 | a0001c0001t0001g0034a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG00408.hp1 HG01255.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-1472dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 13698830 | |||||
chr11:13698845
|
A | G | 9 | a0001c0001t0002g0042a0001c0001t0003g0010a0001c0001t0003g0041others(6): Show | 10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-1472A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698845 | ||||||
chr11:13698847
|
C | A | 4 | a0001c0001t0003g0224a0001c0001t0003g0233a0001c0001t0003g0242others(1): Show | 4 | NA18965.hp1 NA19009.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-1470C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698847 | ||||||
chr11:13698905
|
A | G | 8 | a0001c0001t0003g0027a0001c0001t0006g0004a0001c0001t0006g0028others(5): Show | 10 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.190-1412A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698905 | ||||||
chr11:13698921
|
G | T | 1 | a0001c0001t0003g0242 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.190-1396G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13698921 | ||||||
chr11:13699071
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0012g0129 | 2 | NA18984.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-1246T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699071 | ||||||
chr11:13699121
|
A | G | 4 | a0001c0001t0003g0021a0001c0001t0009g0255a0001c0001t0009g0258others(1): Show | 5 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-1196A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699121 | ||||||
chr11:13699512
|
A | T | 1 | a0001c0001t0001g0032 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.190-805A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699512 | ||||||
chr11:13699930
|
A | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-387A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13699930 | ||||||
chr11:13700312
|
G | T | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.190-5G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 2/11 | chr11 | 13700312 | ||||||
chr11:13700651
|
C | CTCT | 157 | a0001c0001t0001g0085a0001c0001t0002g0025a0001c0001t0002g0168others(154): Show | 169 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.365+169_365+171dup others(3): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13700651 | |||||
chr11:13700692
|
A | G | 2 | a0001c0001t0003g0213a0001c0001t0003g0308 | 2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.365+200A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13700692 | ||||||
chr11:13700842
|
T | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+350T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13700842 | ||||||
chr11:13700937
|
CAA | C | 13 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0256others(10): Show | 15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.365+447_365+448del others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13700937 | |||||
chr11:13700989
|
T | G | 6 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0003g0243others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+497T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13700989 | ||||||
chr11:13701019
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.365+527C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701019 | ||||||
chr11:13701133
|
A | T | 77 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(74): Show | 86 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.365+641A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701133 | ||||||
chr11:13701285
|
TGCTC | T | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+794_365+797del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701285 | ||||||
chr11:13701378
|
A | G | 2 | a0001c0001t0004g0296a0001c0001t0018g0302 | 2 | HG01261.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.365+886A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701378 | ||||||
chr11:13701496
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.365+1004C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701496 | ||||||
chr11:13701605
|
G | A | 1 | a0001c0001t0004g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.365+1113G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701605 | ||||||
chr11:13701919
|
T | C | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.365+1427T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701919 | ||||||
chr11:13701950
|
G | T | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.365+1458G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701950 | ||||||
chr11:13701959
|
C | T | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+1467C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13701959 | ||||||
chr11:13702198
|
C | G | 49 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(46): Show | 53 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.365+1706C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702198 | ||||||
chr11:13702561
|
A | G | 5 | a0001c0001t0004g0283a0001c0001t0004g0295a0001c0001t0004g0303others(2): Show | 5 | HG00544.hp2 NA18953.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+2069A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702561 | ||||||
chr11:13702565
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.365+2073A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702565 | ||||||
chr11:13702682
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+2190A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702682 | ||||||
chr11:13702735
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.365+2243G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13702735 | ||||||
chr11:13703025
|
C | T | 64 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0082others(61): Show | 75 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.365+2533C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703025 | ||||||
chr11:13703044
|
A | G | 1 | a0001c0001t0030g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.365+2552A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703044 | ||||||
chr11:13703111
|
C | T | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.365+2619C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703111 | ||||||
chr11:13703168
|
G | GTTTGTT | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.365+2702_365+2707d others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703168 | |||||
chr11:13703168
|
GTTTGTT | G | 8 | a0001c0001t0002g0025a0001c0001t0002g0246a0001c0001t0003g0226others(5): Show | 9 | HG00621.hp2 HG02080.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.365+2702_365+2707d others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703168 | |||||
chr11:13703168
|
GTTTGTTT others(5): Show |
G | 3 | a0001c0001t0003g0169a0001c0001t0003g0222a0001c0001t0003g0230 | 3 | NA18940.hp2 NA18962.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.365+2696_365+2707d others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703168 | |||||
chr11:13703205
|
A | G | 2 | a0001c0001t0003g0202a0001c0001t0003g0221 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.365+2713A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703205 | ||||||
chr11:13703242
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+2750G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703242 | ||||||
chr11:13703269
|
G | A | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0207others(3): Show | 8 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+2777G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703269 | ||||||
chr11:13703386
|
C | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+2894C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703386 | ||||||
chr11:13703394
|
C | G | 5 | a0001c0001t0002g0017a0001c0001t0002g0052a0001c0001t0002g0053others(2): Show | 6 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+2902C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703394 | ||||||
chr11:13703397
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+2905T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703397 | ||||||
chr11:13703405
|
CTTG | C | 52 | a0001c0001t0002g0208a0001c0001t0002g0246a0001c0001t0003g0019others(49): Show | 54 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.365+2916_365+2918d others(5): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703405 | |||||
chr11:13703452
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.365+2960T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703452 | ||||||
chr11:13703611
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.365+3119A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703611 | ||||||
chr11:13703669
|
G | C | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.365+3177G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703669 | ||||||
chr11:13703740
|
TACTG | T | 4 | a0001c0001t0002g0172a0001c0001t0002g0178a0001c0001t0002g0179others(1): Show | 4 | NA18942.hp2 NA18966.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+3251_365+3254d others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13703740 | |||||
chr11:13703781
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.365+3289C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703781 | ||||||
chr11:13703888
|
A | G | 2 | a0001c0001t0009g0258a0001c0001t0009g0259 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.365+3396A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703888 | ||||||
chr11:13703940
|
A | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.365+3448A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703940 | ||||||
chr11:13703993
|
A | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.365+3501A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703993 | ||||||
chr11:13703993
|
A | G | 45 | a0001c0001t0003g0003a0001c0001t0003g0263a0001c0001t0003g0264others(42): Show | 50 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.365+3501A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13703993 | ||||||
chr11:13704044
|
C | CA | 9 | a0001c0001t0001g0074a0001c0001t0001g0133a0001c0001t0003g0027others(6): Show | 11 | HG01884.hp1 HG01981.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.365+3572dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13704044 | |||||
chr11:13704044
|
CA | C | 92 | a0001c0001t0001g0147a0001c0001t0002g0190a0001c0001t0002g0208others(89): Show | 96 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.365+3572delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13704044 | |||||
chr11:13704288
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.366-3612C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704288 | ||||||
chr11:13704465
|
CTTAAGAA others(2): Show |
C | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-3434_366-3426d others(11): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704465 | ||||||
chr11:13704542
|
G | A | 4 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0228others(1): Show | 4 | NA18942.hp1 NA18982.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-3358G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704542 | ||||||
chr11:13704735
|
TA | T | 35 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(32): Show | 36 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.366-3157delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13704735 | |||||
chr11:13704765
|
C | G | 3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196 | 3 | HG02145.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.366-3135C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704765 | ||||||
chr11:13704944
|
G | A | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.366-2956G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13704944 | ||||||
chr11:13705146
|
C | T | 1 | a0001c0001t0004g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.366-2754C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705146 | ||||||
chr11:13705274
|
AGTCTGAA others(1): Show |
A | 4 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(1): Show | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-2622_366-2615d others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13705274 | |||||
chr11:13705287
|
A | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.366-2613A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705287 | ||||||
chr11:13705362
|
C | G | 54 | a0001c0001t0003g0003a0001c0001t0003g0263a0001c0001t0003g0264others(51): Show | 61 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.366-2538C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705362 | ||||||
chr11:13705363
|
T | G | 156 | a0001c0001t0002g0025a0001c0001t0002g0172a0001c0001t0002g0174others(153): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.366-2537T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705363 | ||||||
chr11:13705533
|
C | T | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-2367C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705533 | ||||||
chr11:13705659
|
C | G | 1 | a0001c0001t0002g0183 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.366-2241C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705659 | ||||||
chr11:13705726
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.366-2174A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705726 | ||||||
chr11:13705759
|
C | G | 50 | a0001c0001t0002g0208a0001c0001t0002g0246a0001c0001t0003g0019others(47): Show | 52 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.366-2141C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705759 | ||||||
chr11:13705936
|
G | A | 1 | a0001c0001t0002g0025 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.366-1964G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13705936 | ||||||
chr11:13706074
|
CT | C | 5 | a0001c0001t0003g0227a0001c0001t0008g0217a0001c0001t0008g0218others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-1819delT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13706074 | |||||
chr11:13706183
|
CAT | C | 5 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1715_366-1714d others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 13706183 | |||||
chr11:13706253
|
T | A | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1647T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706253 | ||||||
chr11:13706464
|
A | G | 159 | a0001c0001t0002g0017a0001c0001t0002g0025a0001c0001t0002g0101others(156): Show | 172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.366-1436A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706464 | ||||||
chr11:13706465
|
T | A | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.366-1435T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706465 | ||||||
chr11:13706469
|
G | A | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.366-1431G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706469 | ||||||
chr11:13706689
|
C | G | 1 | a0001c0001t0002g0099 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.366-1211C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706689 | ||||||
chr11:13706849
|
T | G | 4 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0002g0122others(1): Show | 4 | NA18952.hp2 NA18980.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1051T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13706849 | ||||||
chr11:13707007
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.366-893C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707007 | ||||||
chr11:13707102
|
T | G | 1 | a0001c0005t0003g0267 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.366-798T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707102 | ||||||
chr11:13707287
|
T | A | 5 | a0001c0001t0015g0253a0001c0001t0015g0254a0001c0002t0010g0198others(2): Show | 5 | HG00642.hp1 HG02738.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-613T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707287 | ||||||
chr11:13707494
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.366-406A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707494 | ||||||
chr11:13707669
|
T | G | 3 | a0001c0001t0011g0278a0001c0001t0011g0279a0001c0001t0011g0280 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.366-231T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707669 | ||||||
chr11:13707670
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366-230A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707670 | ||||||
chr11:13707757
|
T | C | 1 | a0001c0001t0001g0034 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.366-143T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 3/11 | chr11 | 13707757 | ||||||
chr11:13708092
|
G | A | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.545+13G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708092 | ||||||
chr11:13708093
|
A | T | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.545+14A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708093 | ||||||
chr11:13708259
|
G | A | 1 | a0001c0001t0005g0192 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545+180G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708259 | ||||||
chr11:13708315
|
G | A | 2 | a0001c0001t0002g0052a0001c0001t0003g0205 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.545+236G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708315 | ||||||
chr11:13708372
|
C | CA | 12 | a0001c0001t0001g0070a0001c0001t0001g0134a0001c0001t0002g0105others(9): Show | 13 | HG00741.hp1 HG01109.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.545+303dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708372 | |||||
chr11:13708432
|
T | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.545+353T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708432 | ||||||
chr11:13708434
|
T | TGC | 29 | a0001c0001t0001g0070a0001c0001t0002g0172a0001c0001t0002g0175others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.545+368_545+369dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708434 | |||||
chr11:13708434
|
T | TGCGC | 6 | a0001c0001t0001g0074a0001c0001t0002g0188a0001c0001t0003g0226others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.545+366_545+369dup others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708434 | |||||
chr11:13708434
|
T | TGCGCGC | 3 | a0001c0001t0003g0043a0001c0001t0006g0004a0001c0001t0008g0217 | 5 | HG02280.hp1 HG02970.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+364_545+369dup others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708434 | |||||
chr11:13708445
|
G | A | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.545+366G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708445 | ||||||
chr11:13708446
|
C | T | 1 | a0001c0001t0004g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.545+367C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708446 | ||||||
chr11:13708447
|
G | A | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.545+368G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708447 | ||||||
chr11:13708447
|
G | GCA | 32 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0015others(29): Show | 34 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.545+397_545+398dup others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCACA | 11 | a0001c0001t0001g0056a0001c0001t0001g0075a0001c0001t0001g0076others(8): Show | 12 | HG01891.hp1 HG02080.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.545+395_545+398dup others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCACACA | 2 | a0001c0001t0001g0014a0001c0001t0013g0199 | 3 | HG03017.hp2 HG03491.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.545+393_545+398dup others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCACACAC others(1): Show |
3 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0013g0200 | 3 | HG02145.hp2 HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.545+391_545+398dup others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0005g0192 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.545+387_545+398dup others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCA | 30 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0131others(27): Show | 32 | HG01069.hp1 HG01243.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACA | 11 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 11 | HG01081.hp2 HG01978.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(1): Show |
18 | a0001c0001t0003g0019a0001c0001t0003g0206a0001c0001t0003g0207others(15): Show | 20 | HG00733.hp2 HG01167.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(3): Show |
8 | a0001c0001t0004g0270a0001c0001t0004g0271a0001c0001t0004g0289others(5): Show | 8 | HG01106.hp2 HG03927.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(5): Show |
8 | a0001c0001t0004g0024a0001c0001t0004g0277a0001c0001t0004g0282others(5): Show | 9 | HG01167.hp2 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(7): Show |
4 | a0001c0001t0004g0276a0001c0001t0004g0285a0001c0001t0004g0300others(1): Show | 4 | HG01070.hp2 HG02738.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(9): Show |
1 | a0001c0001t0015g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.545+369_545+370ins others(16): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(11): Show |
3 | a0001c0001t0004g0299a0001c0001t0011g0278a0001c0001t0011g0280 | 3 | HG01168.hp2 HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.545+369_545+370ins others(18): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCACAC others(13): Show |
2 | a0001c0001t0003g0193a0001c0001t0011g0279 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.545+369_545+370ins others(20): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCGCAC others(1): Show |
4 | a0001c0001t0001g0144a0001c0001t0003g0239a0001c0001t0006g0029others(1): Show | 4 | HG01934.hp2 HG02895.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCGCAC others(3): Show |
4 | a0001c0001t0003g0027a0001c0001t0003g0169a0001c0001t0003g0222others(1): Show | 4 | HG00544.hp2 HG01884.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.545+369_545+370ins others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCGCAC others(7): Show |
1 | a0001c0001t0004g0268 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.545+369_545+370ins others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
G | GCGCGCGC others(5): Show |
1 | a0001c0001t0003g0230 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.545+369_545+370ins others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
GCA | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0079others(7): Show | 11 | HG00642.hp2 HG01515.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.545+397_545+398del others(2): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708447
|
GCACA | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0031others(27): Show | 34 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.545+395_545+398del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708447 | |||||
chr11:13708449
|
A | G | 17 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0002g0042others(14): Show | 18 | HG00639.hp1 HG00735.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.545+370A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708449 | ||||||
chr11:13708451
|
A | G | 12 | a0001c0001t0001g0126a0001c0001t0001g0132a0001c0001t0001g0153others(9): Show | 13 | HG00639.hp1 HG02083.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.545+372A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708451 | ||||||
chr11:13708453
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.545+374A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708453 | ||||||
chr11:13708468
|
CACACACA others(7): Show |
C | 2 | a0001c0001t0003g0257a0001c0001t0003g0265 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.545+390_545+403del others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708468 | ||||||
chr11:13708470
|
CACACACA others(5): Show |
C | 1 | a0001c0001t0003g0260 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.545+392_545+403del others(12): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708470 | ||||||
chr11:13708472
|
CACACATA others(3): Show |
C | 10 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(7): Show | 15 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.545+394_545+403del others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708472 | ||||||
chr11:13708474
|
CACAT | C | 2 | a0001c0001t0002g0017a0001c0001t0002g0107 | 3 | HG02258.hp1 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.545+400_545+403del others(4): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13708474 | |||||
chr11:13708478
|
T | C | 44 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(41): Show | 46 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.545+399T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708478 | ||||||
chr11:13708728
|
C | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.545+649C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708728 | ||||||
chr11:13708911
|
G | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0001t0001g0132others(2): Show | 5 | NA18964.hp2 NA18980.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+832G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13708911 | ||||||
chr11:13709057
|
A | G | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.545+978A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709057 | ||||||
chr11:13709134
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02165.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.545+1055T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709134 | ||||||
chr11:13709252
|
T | TA | 4 | a0001c0001t0005g0023a0001c0001t0005g0273a0001c0001t0005g0274others(1): Show | 5 | HG02486.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.545+1181dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 13709252 | |||||
chr11:13709328
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.545+1249G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709328 | ||||||
chr11:13709331
|
C | G | 2 | a0001c0001t0004g0284a0001c0001t0004g0288 | 2 | HG01167.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.545+1252C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709331 | ||||||
chr11:13709351
|
TC | T | 7 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0063others(4): Show | 9 | HG00140.hp2 HG00735.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.545+1273delC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709351 | ||||||
chr11:13709388
|
C | T | 158 | a0001c0001t0001g0074a0001c0001t0002g0025a0001c0001t0002g0106others(155): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.546-1305C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709388 | ||||||
chr11:13709415
|
G | A | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.546-1278G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709415 | ||||||
chr11:13709524
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546-1169G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709524 | ||||||
chr11:13709702
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.546-991A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709702 | ||||||
chr11:13709790
|
T | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.546-903T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709790 | ||||||
chr11:13709839
|
A | C | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.546-854A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709839 | ||||||
chr11:13709899
|
T | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.546-794T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709899 | ||||||
chr11:13709928
|
C | A | 13 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0256others(10): Show | 15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.546-765C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709928 | ||||||
chr11:13709969
|
A | G | 1 | a0001c0001t0003g0247 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546-724A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13709969 | ||||||
chr11:13710069
|
T | C | 20 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0175others(17): Show | 20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.546-624T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710069 | ||||||
chr11:13710081
|
C | T | 4 | a0001c0001t0003g0021a0001c0001t0009g0255a0001c0001t0009g0258others(1): Show | 5 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-612C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710081 | ||||||
chr11:13710095
|
A | G | 55 | a0001c0001t0001g0074a0001c0001t0002g0106a0001c0001t0002g0208others(52): Show | 57 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.546-598A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710095 | ||||||
chr11:13710383
|
A | G | 2 | a0001c0001t0003g0227a0001c0001t0003g0252 | 2 | NA18939.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.546-310A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710383 | ||||||
chr11:13710464
|
G | T | 2 | a0001c0001t0004g0284a0001c0001t0004g0288 | 2 | HG01167.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.546-229G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710464 | ||||||
chr11:13710466
|
A | G | 4 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(1): Show | 4 | HG00735.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-227A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 4/11 | chr11 | 13710466 | ||||||
chr11:13710987
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.723+117C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 5/11 | chr11 | 13710987 | ||||||
chr11:13711010
|
A | C | 1 | a0001c0001t0002g0025 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.723+140A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 5/11 | chr11 | 13711010 | ||||||
chr11:13711854
|
C | T | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.768+46C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 6/11 | chr11 | 13711854 | ||||||
chr11:13711904
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.769-24G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 6/11 | chr11 | 13711904 | ||||||
chr11:13712134
|
A | G | 1 | a0001c0001t0003g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.887+88A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712134 | ||||||
chr11:13712150
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.887+104A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712150 | ||||||
chr11:13712291
|
G | GA | 18 | a0001c0001t0002g0025a0001c0001t0003g0027a0001c0001t0003g0312others(15): Show | 21 | HG00642.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.887+258dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 13712291 | |||||
chr11:13712525
|
A | G | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.888-441A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712525 | ||||||
chr11:13712535
|
TTGATAAT others(10): Show |
T | 4 | a0001c0001t0003g0027a0001c0001t0006g0004a0001c0001t0006g0028others(1): Show | 6 | HG01884.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-428_888-412del others(17): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 13712535 | |||||
chr11:13712542
|
T | C | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-424T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712542 | ||||||
chr11:13712703
|
A | T | 1 | a0001c0001t0004g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.888-263A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | chr11 | 13712703 | ||||||
chr11:13712763
|
GTTA | G | 4 | a0001c0001t0003g0003a0001c0001t0003g0045a0001c0001t0003g0263others(1): Show | 7 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.888-197_888-195del others(3): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 13712763 | |||||
chr11:13713131
|
A | T | 1 | a0001c0001t0003g0306 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.955+98A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713131 | ||||||
chr11:13713132
|
C | A | 1 | a0001c0001t0003g0306 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.955+99C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713132 | ||||||
chr11:13713293
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.955+260C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713293 | ||||||
chr11:13713323
|
T | A | 8 | a0001c0001t0003g0027a0001c0001t0006g0004a0001c0001t0006g0028others(5): Show | 10 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.955+290T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713323 | ||||||
chr11:13713520
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.955+487C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713520 | ||||||
chr11:13713794
|
G | C | 1 | a0001c0001t0002g0025 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.956-715G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713794 | ||||||
chr11:13713831
|
A | G | 19 | a0001c0001t0001g0036a0001c0001t0001g0081a0001c0001t0001g0123others(16): Show | 19 | HG00280.hp2 HG00621.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-678A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713831 | ||||||
chr11:13713920
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.956-589T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713920 | ||||||
chr11:13713927
|
T | C | 1 | a0001c0001t0004g0289 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.956-582T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713927 | ||||||
chr11:13713948
|
G | A | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-561G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13713948 | ||||||
chr11:13714154
|
TA | T | 9 | a0001c0001t0002g0042a0001c0001t0003g0010a0001c0001t0003g0041others(6): Show | 10 | HG00639.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-353delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 13714154 | |||||
chr11:13714187
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.956-322G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714187 | ||||||
chr11:13714195
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.956-314C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714195 | ||||||
chr11:13714371
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.956-138T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714371 | ||||||
chr11:13714410
|
T | A | 1 | a0001c0001t0003g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.956-99T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 8/11 | chr11 | 13714410 | ||||||
chr11:13714843
|
G | A | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1127+163G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13714843 | ||||||
chr11:13714906
|
C | A | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+226C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13714906 | ||||||
chr11:13714997
|
T | G | 1 | a0001c0001t0003g0203 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1127+317T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13714997 | ||||||
chr11:13715124
|
T | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1127+444T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13715124 | ||||||
chr11:13715746
|
C | T | 6 | a0001c0001t0005g0023a0001c0001t0005g0269a0001c0001t0005g0273others(3): Show | 7 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+1066C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13715746 | ||||||
chr11:13715957
|
T | C | 20 | a0001c0001t0002g0172a0001c0001t0002g0174a0001c0001t0002g0175others(17): Show | 20 | HG00323.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1127+1277T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13715957 | ||||||
chr11:13716061
|
A | G | 1 | a0001c0001t0003g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1127+1381A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716061 | ||||||
chr11:13716168
|
A | G | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1127+1488A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716168 | ||||||
chr11:13716227
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1127+1547T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716227 | ||||||
chr11:13716304
|
T | C | 52 | a0001c0001t0003g0003a0001c0001t0003g0263a0001c0001t0003g0264others(49): Show | 59 | HG00544.hp2 HG00733.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1127+1624T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716304 | ||||||
chr11:13716485
|
T | C | 1 | a0001c0001t0004g0290 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1127+1805T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716485 | ||||||
chr11:13716533
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1127+1853C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716533 | ||||||
chr11:13716684
|
G | A | 310 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(307): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1127+2004G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716684 | ||||||
chr11:13716803
|
T | A | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1127+2123T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716803 | ||||||
chr11:13716900
|
T | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1127+2220T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716900 | ||||||
chr11:13716941
|
C | G | 2 | a0001c0001t0003g0202a0001c0001t0003g0221 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1127+2261C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13716941 | ||||||
chr11:13717059
|
A | G | 1 | a0001c0001t0003g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1127+2379A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717059 | ||||||
chr11:13717063
|
T | G | 1 | a0001c0001t0003g0169 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1127+2383T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717063 | ||||||
chr11:13717074
|
AC | A | 4 | a0001c0001t0007g0194a0001c0001t0007g0195a0001c0001t0007g0196others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+2396delC | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 13717074 | |||||
chr11:13717119
|
A | G | 3 | a0001c0001t0003g0022a0001c0001t0003g0261a0001c0001t0003g0262 | 4 | HG01884.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+2439A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717119 | ||||||
chr11:13717201
|
T | C | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1127+2521T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717201 | ||||||
chr11:13717367
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1127+2687A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717367 | ||||||
chr11:13717614
|
C | T | 3 | a0001c0001t0003g0233a0001c0001t0003g0242a0001c0001t0003g0245 | 3 | NA18965.hp1 NA19009.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1127+2934C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13717614 | ||||||
chr11:13718009
|
T | C | 77 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(74): Show | 86 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1127+3329T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718009 | ||||||
chr11:13718032
|
A | G | 1 | a0001c0001t0004g0282 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1127+3352A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718032 | ||||||
chr11:13718286
|
A | G | 19 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(16): Show | 24 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1128-3444A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718286 | ||||||
chr11:13718359
|
A | G | 1 | a0001c0001t0003g0240 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1128-3371A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718359 | ||||||
chr11:13718510
|
C | T | 1 | a0001c0001t0002g0017 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1128-3220C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718510 | ||||||
chr11:13718827
|
G | C | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-2903G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13718827 | ||||||
chr11:13719248
|
T | G | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1128-2482T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719248 | ||||||
chr11:13719714
|
A | C | 1 | a0001c0007t0002g0165 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1128-2016A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719714 | ||||||
chr11:13719728
|
G | A | 5 | a0001c0001t0008g0217a0001c0001t0008g0218a0001c0001t0008g0219others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128-2002G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719728 | ||||||
chr11:13719923
|
A | C | 26 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(23): Show | 33 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1128-1807A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719923 | ||||||
chr11:13719939
|
A | G | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | NA18964.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1128-1791A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13719939 | ||||||
chr11:13720035
|
C | G | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG00408.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1128-1695C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720035 | ||||||
chr11:13720073
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1128-1657A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720073 | ||||||
chr11:13720346
|
C | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1128-1384C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720346 | ||||||
chr11:13720536
|
T | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1128-1194T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720536 | ||||||
chr11:13720553
|
T | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1128-1177T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720553 | ||||||
chr11:13720650
|
A | AT | 30 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 33 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1128-1073dupT | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 13720650 | |||||
chr11:13720660
|
CCTT | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0141others(2): Show | 6 | HG01069.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1128-1069_1128-106 others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720660 | ||||||
chr11:13720703
|
A | G | 1 | a0001c0001t0007g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1128-1027A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720703 | ||||||
chr11:13720754
|
T | C | 1 | a0001c0001t0003g0204 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1128-976T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13720754 | ||||||
chr11:13721016
|
A | G | 5 | a0001c0001t0002g0017a0001c0001t0002g0052a0001c0001t0002g0053others(2): Show | 6 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1128-714A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721016 | ||||||
chr11:13721030
|
G | A | 1 | a0001c0001t0004g0292 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1128-700G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721030 | ||||||
chr11:13721257
|
G | C | 73 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(70): Show | 82 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1128-473G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721257 | ||||||
chr11:13721284
|
G | A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1128-446G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721284 | ||||||
chr11:13721287
|
TTATAAA | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1128-437_1128-432d others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 13721287 | |||||
chr11:13721638
|
A | G | 6 | a0001c0001t0005g0023a0001c0001t0005g0269a0001c0001t0005g0273others(3): Show | 7 | HG02559.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1128-92A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 9/11 | chr11 | 13721638 | ||||||
chr11:13721957
|
A | G | 1 | a0001c0001t0026g0201 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257+98A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13721957 | ||||||
chr11:13722005
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0114 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1257+146G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722005 | ||||||
chr11:13722010
|
T | C | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+151T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722010 | ||||||
chr11:13722261
|
C | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+402C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722261 | ||||||
chr11:13722574
|
A | G | 1 | a0001c0001t0004g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1257+715A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722574 | ||||||
chr11:13722576
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1257+717C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722576 | ||||||
chr11:13722662
|
C | T | 2 | a0001c0001t0004g0268a0001c0001t0004g0299 | 2 | HG01168.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1257+803C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722662 | ||||||
chr11:13722843
|
C | CCT | 53 | a0001c0001t0001g0160a0001c0001t0002g0001a0001c0001t0002g0002others(50): Show | 63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1257+999_1257+1000 others(5): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | |||||
chr11:13722843
|
C | CCTCT | 12 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0256others(9): Show | 16 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1257+997_1257+1000 others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | |||||
chr11:13722843
|
C | CCTCTCT | 2 | a0001c0001t0003g0022a0001c0001t0003g0262 | 3 | HG02145.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1257+995_1257+1000 others(9): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | |||||
chr11:13722843
|
C | CCTCTCTC others(3): Show |
29 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(26): Show | 31 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.1257+991_1257+1000 others(13): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | |||||
chr11:13722843
|
C | CCTCTCTC others(5): Show |
5 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0004g0288others(2): Show | 5 | HG01167.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+989_1257+1000 others(15): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722843 | |||||
chr11:13722858
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0011g0280 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1257+1000_1257+100 others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | |||||
chr11:13722858
|
C | CTCTCTCT others(3): Show |
4 | a0001c0001t0004g0275a0001c0001t0004g0290a0001c0001t0011g0278others(1): Show | 4 | HG02027.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+1000_1257+100 others(14): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | |||||
chr11:13722858
|
C | CTCTCTCT others(5): Show |
1 | a0001c0001t0005g0301 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1257+1000_1257+100 others(16): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | |||||
chr11:13722858
|
C | CTCTCTCT others(5): Show |
2 | a0001c0001t0004g0277a0001c0001t0005g0192 | 2 | HG02622.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1257+1000_1257+100 others(16): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | |||||
chr11:13722858
|
CTATA | C | 45 | a0001c0001t0002g0246a0001c0001t0003g0019a0001c0001t0003g0020others(42): Show | 47 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1257+1016_1257+101 others(8): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13722858 | |||||
chr11:13722860
|
A | C | 187 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1257+1001A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722860 | ||||||
chr11:13722862
|
A | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0031others(57): Show | 68 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1257+1003A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722862 | ||||||
chr11:13722864
|
A | C | 5 | a0001c0001t0001g0167a0001c0001t0002g0181a0001c0001t0003g0241others(2): Show | 5 | HG00423.hp1 HG02080.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+1005A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13722864 | ||||||
chr11:13723006
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0054 | 3 | HG00597.hp2 HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1257+1147T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723006 | ||||||
chr11:13723186
|
G | A | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1257+1327G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723186 | ||||||
chr11:13723256
|
T | C | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+1397T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723256 | ||||||
chr11:13723290
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1257+1431G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723290 | ||||||
chr11:13723351
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257+1492T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723351 | ||||||
chr11:13723362
|
C | CA | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1257+1524dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13723362 | |||||
chr11:13723362
|
C | CAA | 23 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0074others(20): Show | 23 | HG00621.hp1 HG00621.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1257+1523_1257+152 others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13723362 | |||||
chr11:13723362
|
CA | C | 36 | a0001c0001t0001g0069a0001c0001t0002g0115a0001c0001t0002g0187others(33): Show | 38 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1257+1524delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13723362 | |||||
chr11:13723380
|
A | C | 1 | a0001c0001t0007g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1257+1521A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723380 | ||||||
chr11:13723384
|
C | A | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+1525C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723384 | ||||||
chr11:13723388
|
A | C | 41 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(38): Show | 43 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1257+1529A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723388 | ||||||
chr11:13723389
|
A | C | 2 | a0001c0001t0004g0276a0001c0001t0004g0300 | 2 | HG02738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1257+1530A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723389 | ||||||
chr11:13723411
|
T | G | 42 | a0001c0001t0004g0024a0001c0001t0004g0026a0001c0001t0004g0268others(39): Show | 44 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1257+1552T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723411 | ||||||
chr11:13723739
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1257+1880G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13723739 | ||||||
chr11:13724226
|
G | A | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+2367G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724226 | ||||||
chr11:13724274
|
G | GTACTAC | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1257+2416_1257+241 others(10): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724274 | |||||
chr11:13724276
|
G | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1257+2417G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724276 | ||||||
chr11:13724277
|
G | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(13): Show | 21 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1257+2418G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724277 | ||||||
chr11:13724335
|
C | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0063a0001c0001t0002g0112others(1): Show | 6 | HG00140.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1257+2476C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724335 | ||||||
chr11:13724371
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1257+2512C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724371 | ||||||
chr11:13724398
|
A | G | 1 | a0001c0001t0006g0028 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1257+2539A>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724398 | ||||||
chr11:13724549
|
CA | C | 10 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0001g0162others(7): Show | 10 | HG00323.hp2 HG00741.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1257+2710delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724549 | |||||
chr11:13724549
|
CAA | C | 258 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(255): Show | 290 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.1257+2709_1257+271 others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724549 | |||||
chr11:13724549
|
CAAA | C | 48 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0169others(45): Show | 50 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1257+2708_1257+271 others(7): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13724549 | |||||
chr11:13724645
|
C | G | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1257+2786C>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724645 | ||||||
chr11:13724776
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0002g0191a0001c0001t0029g0173 | 3 | HG00323.hp1 HG01069.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1258-2780C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724776 | ||||||
chr11:13724781
|
A | C | 1 | a0001c0001t0003g0207 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1258-2775A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724781 | ||||||
chr11:13724833
|
G | T | 1 | a0001c0001t0007g0197 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1258-2723G>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13724833 | ||||||
chr11:13725175
|
A | T | 1 | a0001c0001t0003g0213 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1258-2381A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725175 | ||||||
chr11:13725294
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0114 | 2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1258-2262T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725294 | ||||||
chr11:13725349
|
T | A | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1258-2207T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725349 | ||||||
chr11:13725443
|
TA | T | 104 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0020others(101): Show | 113 | HG00140.hp1 HG00544.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.1258-2097delA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13725443 | |||||
chr11:13725443
|
TAA | T | 16 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0213others(13): Show | 18 | HG00280.hp1 HG01081.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.1258-2098_1258-209 others(6): Show |
FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13725443 | |||||
chr11:13725617
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1258-1939G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725617 | ||||||
chr11:13725853
|
C | A | 2 | a0001c0001t0015g0253a0001c0001t0015g0254 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1258-1703C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725853 | ||||||
chr11:13725867
|
T | G | 1 | a0001c0001t0002g0025 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1258-1689T>G | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13725867 | ||||||
chr11:13726114
|
C | A | 4 | a0001c0001t0001g0127a0001c0002t0010g0198a0001c0002t0010g0310others(1): Show | 4 | HG00642.hp1 HG01993.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-1442C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726114 | ||||||
chr11:13726116
|
G | A | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1258-1440G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726116 | ||||||
chr11:13726121
|
T | C | 1 | a0001c0001t0003g0313 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1258-1435T>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726121 | ||||||
chr11:13726245
|
C | T | 2 | a0001c0001t0014g0073a0001c0001t0014g0163 | 2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1258-1311C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726245 | ||||||
chr11:13726257
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1258-1299C>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726257 | ||||||
chr11:13726639
|
G | A | 2 | a0001c0001t0013g0199a0001c0001t0013g0200 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1258-917G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726639 | ||||||
chr11:13726662
|
G | C | 225 | a0001c0001t0001g0127a0001c0001t0002g0001a0001c0001t0002g0002others(222): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1258-894G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726662 | ||||||
chr11:13726741
|
T | A | 68 | a0001c0001t0003g0003a0001c0001t0003g0021a0001c0001t0003g0022others(65): Show | 77 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.1258-815T>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726741 | ||||||
chr11:13726741
|
T | TA | 3 | a0001c0001t0004g0293a0001c0001t0015g0253a0001c0001t0015g0254 | 3 | HG02886.hp1 HG03540.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1258-812dupA | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr11 | 13726741 | |||||
chr11:13726992
|
G | A | 3 | a0001c0001t0004g0303a0001c0001t0004g0304a0001c0001t0004g0305 | 3 | NA18953.hp2 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1258-564G>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13726992 | ||||||
chr11:13727340
|
G | C | 3 | a0001c0002t0010g0198a0001c0002t0010g0310a0002c0003t0010g0311 | 3 | HG00642.hp1 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1258-216G>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 10/11 | chr11 | 13727340 | ||||||
chr11:13727900
|
C | A | 3 | a0001c0001t0006g0004a0001c0001t0006g0028a0001c0001t0006g0029 | 5 | HG02809.hp2 HG02895.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1385+217C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13727900 | ||||||
chr11:13728044
|
A | C | 1 | a0001c0001t0003g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1385+361A>C | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13728044 | ||||||
chr11:13728369
|
A | T | 13 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0256others(10): Show | 15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1386-243A>T | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13728369 | ||||||
chr11:13728499
|
C | A | 52 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0092others(49): Show | 54 | HG00140.hp1 HG00621.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.1386-113C>A | FAR1 | ENSG00000197601.14 | transcript | ENST00000354817.8 | protein_coding | 11/11 | chr11 | 13728499 |